EP0228003A1 - Preparation of a multilayer coating - Google Patents

Preparation of a multilayer coating Download PDF

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Publication number
EP0228003A1
EP0228003A1 EP86117295A EP86117295A EP0228003A1 EP 0228003 A1 EP0228003 A1 EP 0228003A1 EP 86117295 A EP86117295 A EP 86117295A EP 86117295 A EP86117295 A EP 86117295A EP 0228003 A1 EP0228003 A1 EP 0228003A1
Authority
EP
European Patent Office
Prior art keywords
groups
isocyanate groups
base coating
coating composition
resin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP86117295A
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German (de)
French (fr)
Other versions
EP0228003B1 (en
EP0228003B2 (en
Inventor
Hans Dieter Hille
Franz Ebner
Hermann-Josef Dr. Drexler
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BASF Farben und Fasern AG
Original Assignee
BASF Lacke und Farben AG
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Application filed by BASF Lacke und Farben AG filed Critical BASF Lacke und Farben AG
Priority to AT86117295T priority Critical patent/ATE51633T1/en
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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/50—Multilayers
    • B05D7/52—Two layers
    • B05D7/53—Base coat plus clear coat type
    • B05D7/532—Base coat plus clear coat type the two layers being cured or baked together, i.e. wet on wet
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
    • C08G18/0819—Manufacture of polymers containing ionic or ionogenic groups containing anionic or anionogenic groups
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—Polyurethanes
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31605—Next to free metal

Definitions

  • Multicoat paint systems are preferably applied according to the so-called "basecoat-clearcoat” process, i.e. a pigmented basecoat is pre-coated and after a short flash-off time without a baking step (wet-on-wet process), overcoated with clearcoat. The basecoat and clearcoat are then baked together.
  • basecoat-clearcoat i.e. a pigmented basecoat is pre-coated and after a short flash-off time without a baking step (wet-on-wet process), overcoated with clearcoat.
  • the basecoat and clearcoat are then baked together.
  • the "basecoat-clearcoat” process has become particularly important in the application of automotive metallic effect paints.
  • metal effect depends crucially on the orientation of the metal pigment particles in the paint film.
  • a metal effect basecoat which can be processed in the "wet-on-wet" process must be used accordingly provide paint films in which the metal pigments are in a favorable spatial orientation after application and in which this orientation is quickly fixed in such a way that it cannot be disturbed in the course of the further painting process.
  • the coating agents disclosed in US 4,558,090 are well suited for the production of the base layer of multi-layer coatings, but they are unsuitable for practical use, especially in series painting processes, because the quick drying coating agents in the application devices used (for example paint spray gun; automatic, electrostatically assisted high-speed rotary systems) etc). stick so well that they can only be removed with great difficulty. As a result, it is not possible to change the applied coating systems (e.g. color change) very quickly, especially in automotive serial painting.
  • aqueous dispersions which can be used as base coating compositions for the production of multilayer protective and / or decorative coatings on substrate surfaces and which meet and also meet all the requirements set out above for a base coating composition the application devices used can be processed without any problems.
  • aqueous dispersions according to the preamble of claim 1, which are characterized in that the polyurethane resin by reacting the intermediate product obtained from (A) and (B) and (C) with an at least three hydroxyl groups Polyol, preferably triol, and transfer of the reaction product thus obtained into the aqueous phase.
  • the dispersions according to the invention are obtained by reacting components (A), (B) and (C) to form an intermediate product containing terminal isocyanate groups.
  • the reaction of components (A), (B) and (C) takes place according to the well-known methods of organic chemistry, preferably a step-by-step reaction of the components (for example formation of a first intermediate product from components (A) and (B), the is then reacted with (C) to form a second intermediate).
  • components (A), (B) and (C) can also be reacted simultaneously.
  • the reaction is preferably carried out in solvents which are inert to isocyanate groups and are miscible with water.
  • Solvents are advantageously used which, in addition to the properties described above, are also good solvents for the polyurethanes produced and can be easily separated from aqueous mixtures. Acetone and methyl ethyl ketone are particularly suitable solvents.
  • Examples are poly (oxytetramethylene) glycols, poly (oxyethylene) glycols and poly (oxypropylene) glycols.
  • the preferred polyalkylene ether polyols are poly (oxypropylene) glycols with a molecular weight in the range of 400 to 3,000.
  • Polyester diols can also be used as the polymeric diol component (component A) in the invention.
  • the polyester diols can be prepared by esterifying organic dicarboxylic acids or their anhydrides with organic diols.
  • the dicarboxylic acids and the diols can be aliphatic or aromatic dicarboxylic acids and diols.
  • the diols used to make the polyesters include alkylene glycols such as ethylene glycol, butylene glycol, neopenty glycol and other glycols such as dimethylolcyclohexane.
  • Suitable acids are, for example, phthalic acid, isophthalic acid, terephthalic acid, tetrahydrophthalic acid, hexahydrophthalic acid, adipic acids, azelaic acid, sebacic acid, maleic acid, glutaric acid, hexachlorheptanedicarboxylic acid and tetrachlorophthalic acid.
  • their anhydrides can also be used these exist.
  • polyester diols derived from lactones can also be used as component (A) in the invention. These products are obtained, for example, by reacting an ⁇ -caprolactone with a diol. Such products are described in U.S. Patent 3,169,945.
  • the polylactone polyols which are obtained by this reaction are distinguished by the presence of a terminal hydroxyl group and by recurring polyester fractions which are derived from the lactone.
  • These recurring molecular parts can be of the formula - - (CHR) n - CH2O - in which n is preferably 4 to 6 and the substituent is hydrogen, an alkyl radical, a cycloalkyl radical or an alkoxy radical, where no substituent contains more than 12 carbon atoms and the total number of carbon atoms in the substituent in the lactone ring does not exceed 12.
  • the lactone used as the starting material can be any lactone or any combination of lactones, which lactone should contain at least 6 carbon atoms in the ring, for example 6 to 8 carbon atoms and where there should be at least 2 hydrogen substituents on the carbon atom attached to the Oxygen group of the ring is bound.
  • the lactone used as a raw material can be represented by the following general formula. in the n and R have the meaning already given.
  • lactones preferred for the preparation of the polyester diols in the invention are the caprolactones, in which n has the value 4.
  • the most preferred lactone is the unsubstituted ⁇ -caprolactone, where n is 4 and all R substituents are hydrogen. This lactone is particularly preferred because it is available in large quantities and gives coatings with excellent properties.
  • various other lactones can be used individually or in combination.
  • aliphatic diols suitable for reaction with the lactone include ethylene glycol, 1,3-propanediol, 1,4-butanediol, dimethylolcyclohexane.
  • Any organic diisocyanates can be used as component (B) for the production of the polyurethane dispersion.
  • suitable diisocyanates are trimethylene diisocyanate, tetramethylene diisocyanate, pentamethylene diisocyanate, hexamethylene diisocyanate, propylene diisocyanate, ethyl ethylene diisocyanate, 2,3-dimethylethylene diisocyanate, 1-methyltrimethylene diisocyanate, 1,3-cyclopentylene diisocyanate, 1,4-cyclohexylene diisocyanate diisocyanate, 1,2-diisocyanate diisocyanate, 1,2-diisocyanate diisocyanate, 1,2-cyclohexylene diisocyanate, 1,2-diisocyanate diisocyanate, 1,2-cyclohexylene diisocyanate, 1,2-diisocyanate diisocyanate, 1,2-cyclohexylene diisocyan
  • Compounds which contain two groups which are reactive toward isocyanate groups are used as component (C), at least some of which are used as components (C) compounds used has at least one group capable of forming anions, which has preferably been neutralized before the reaction with a tertiary amine.
  • the proportion of ionic groups in the polyurethane molecule can be controlled by setting a certain mixing ratio between the groups containing the groups capable of forming anions and the compounds free of these groups.
  • Suitable groups reacting with isocyanate groups are in particular hydroxyl groups.
  • the use of compounds containing primary or secondary amino groups can have a negative impact on the processability of the dispersions described above.
  • the type and amount of any compounds containing amino groups to be used can be determined by the person skilled in the art by means of routine tests which are simple to carry out.
  • Compounds containing amino groups are, for example, ⁇ , ⁇ -diaminovaleric acid, 3,4-diaminobenzoic acid, 2,4-diamino-toluenesulfonic acid- (5), 4,4'-diamino-diphenyl ether sulfonic acid and the like.
  • Suitable tertiary amines for neutralizing the anionic groups are, for example, trimethylamine, triethylamine, dimethylaniline, diethylaniline, triphenylamine and the like.
  • Low molecular weight diols or diamines with primary or secondary amino groups can be used, for example, as compounds which have two groups reactive toward isocyanate groups but are free from groups capable of forming anions.
  • the isocyanate group-containing intermediate formed from (A), (B) and (C) is reacted with the polyol containing at least three hydroxyl groups, which most likely results in chain extension and possibly also branching of the binder molecule.
  • all polyols containing at least three hydroxyl groups which can be reacted with the intermediate product obtained from (A), (B) and (C) in such a way that no crosslinked products are formed, are suitable for producing the polyurethane dispersion according to the invention.
  • examples include trimethylolpropane, glycerol, erythritol, mesoerythritol, arabitol, adonitol, xylitol, mannitol, sorbitol, dulcitol, hexanetriol, (poly) -pentaerythritol, etc.
  • the resulting polyurethane dissolves well and can easily be separated from aqueous mixtures (e.g. acetone or Methyl ethyl ketone) has been carried out and, if necessary, neutralization of the groups capable of forming anions is carried out, the reaction product is converted into an aqueous phase. This can be done, for example, by dispersing the reaction mixture in water and distilling off the organic solvent components boiling below 100 ° C.
  • aqueous mixtures e.g. acetone or Methyl ethyl ketone
  • the aqueous phase is understood to mean water, which can also contain organic solvents.
  • solvents which may be present in water are heterocyclic, aliphatic or aromatic hydrocarbons, mono- or polyhydric alcohols, ethers, esters and ketones, such as, for example, N-methylpyrrolidone, toluene, xylene, butanol, ethyl and butyl glycol and their acetates, butyl diglycol, ethylene glycol dibutyl ether, ethylene glycol diethyl ether, diethylene glycol dimethyl ether, cyclohexanone, methyl ethyl ketone, acetone, isophorone or mixtures thereof.
  • the dispersion forms the basis of the coating compositions according to the invention, into which the other constituents, such as e.g. Additional binders, pigments, organic solvents and auxiliaries can be incorporated homogeneously by dispersing, for example using a stirrer or dissolver.
  • the pH is checked again and, if necessary, adjusted to a value of 6 to 9, preferably 7.0 to 8.5.
  • the solids content and the viscosity are adjusted to the values adapted to the respective application conditions.
  • the ready-to-use coating compositions generally have a solids content of 10 to 30% by weight and their run-out time in the ISO cup 4 is 15 to 30 seconds, preferably 18 to 25 seconds.
  • Their proportion of water is 60 to 90% by weight, that of organic solvents 0 to 20% by weight, in each case based on the total coating agent.
  • the base coating compositions according to the invention advantageously contain, as an additional binder component, a water-dilutable melamine resin in a proportion of 1 to 80% by weight, preferably 20 to 60% by weight, based on the solids content of the polyurethane dispersion.
  • Water-soluble melamine resins are known per se and are used on a larger scale. These are etherified melamine-formaldehyde condensation products. Apart from the degree of condensation, which should be as low as possible, their solubility in water depends on the etherification component, only the lowest members of the alkanol or ethylene glycol monoether series giving water-soluble condensates. Hexamethoxymethylmelamine resins are of the greatest importance. If solubilizers are used, butanol-etherified melamine resins can also be dispersed in the aqueous phase.
  • Transetherification products of highly etherified formaldehyde condensates with oxycarboxylic acids are water-soluble via their carboxyl group after neutralization and can be used as a crosslinking component in the coating compositions according to the invention.
  • melamine resins described instead of the melamine resins described, other water-soluble or water-dispersible amino resins such as e.g. Benzoguanamine resins are used.
  • the base coating composition according to the invention contains a melamine resin
  • it can advantageously additionally contain, as a further binder component, a water-dilutable polyester resin and / or a water-dilutable polyacrylate resin, the weight ratio of melamine resin: polyester / polyacrylate resin being 2: 1 to 1: 4 and the total proportion of melamine resin, polyester / polyacrylate resin, based on the solids content of the polyurethane dispersion, is 1 to 80% by weight, preferably 20 to 60% by weight.
  • Water-dilutable polyesters are those with free carboxyl groups, ie polyesters with a high acid number.
  • the first way is to terminate the esterification at the desired acid number. After neutralization with bases, the polyesters thus obtained are soluble in water and form a film when baked.
  • the second possibility is the formation of partial esters of di- or polycarboxylic acids with hydroxyl-rich polyesters with a low acid number. For this reaction, anhydrides of dicarboxylic acids are usually used, which are reacted with the hydroxyl component under mild conditions to form a free carboxyl group.
  • the water-dilutable polyacrylate resins contain free carboxyl groups. They are usually acrylic or methacrylic copolymers, and the carboxyl groups come from the proportions of acrylic or methacrylic acid.
  • Blocked polyisocyanates can also be used as crosslinking agents. Any polyisocyanates in which the isocyanate groups have been reacted with a compound can be used in the invention, so that the blocked polyisocyanate formed is resistant to hydroxyl groups at room temperature, at elevated temperatures, generally in the range from about 90 to 300 ° C. , but responds. Any organic polyisocyanates suitable for crosslinking can be used in the preparation of the blocked polyisocyanates.
  • the isocyanates which contain about 3 to about 36, in particular about 8 to 15, carbon atoms are preferred. Examples of suitable diisocyanates are the above-mentioned diisocyanates (component B).
  • Polyisocyanates with higher isocyanate functionality can also be used.
  • Examples include tris (4-isocyanatophenyl) methane, 1,3,5-triisocyanatobenzene, 2,4,6-triisocyanatotoluene, 1,3,5-tris (6-iso cyanatohexyl) biuret.
  • the organic polyisocyanates which are suitable as crosslinking agents in the invention can also be prepolymers which are derived, for example, from a polyol, including a polyether polyol or a polyester polyol.
  • a polyol including a polyether polyol or a polyester polyol.
  • polyols are reacted with an excess of polyisocyanates, resulting in prepolymers with terminal isocyanate groups.
  • polyols examples include simple polyols, such as glycols, for example ethylene glycol and propylene glycol, and other polyols, such as glycerol, trimethylolpropane, hexanetriol and pentaerythritol; also monoethers, such as diethylene glycol and dipropylene glycol, and polyethers, which are adducts of such polyols and alkylene oxides.
  • alkylene oxides which are suitable for polyaddition to these polyols to form polyethers are ethylene oxide, propylene oxide, butylene oxide and styrene oxide.
  • polyethers with terminal hydroxyl groups are generally referred to as polyethers with terminal hydroxyl groups. They can be linear or branched. Examples of such polyethers are polyoxyethylene glycol with a molecular weight of 1,540, polyoxypropylene glycol with a molecular weight of 1,025, polyoxytetramethylene glycol, polyoxyhexamethylene glycol, polyoxynonamethylene glycol, polyoxydecamethylene glycol, polyoxydodecamethylene glycol and mixtures thereof. Other types of polyoxyalkylene glycol ethers can also be used.
  • Particularly suitable polyether polyols are those which are obtained by reacting such polyols, such as ethylene glycol, diethylene glycol, triethylene glycol, 1,4-butanediol, 1,3-butanediol, 1,6-hexanediol and mixtures thereof; Glycerol trimethylol ethane, trimethylol propane, 1,2,6-hexanetriol, dipentaerythritol, tripentaerythritol, polypentaerythritol, methyl glucosides and sucrose with alkylene oxides, such as ethylene oxide, propylene oxide or mixtures thereof.
  • alkylene oxides such as ethylene oxide, propylene oxide or mixtures thereof.
  • Any suitable aliphatic, cycloaliphatic or aromatic alkyl mono alcohols can be used to block the polyisocyanates.
  • suitable aliphatic, cycloaliphatic or aromatic alkyl mono alcohols can be used to block the polyisocyanates.
  • aliphatic alcohols such as methyl, ethyl, chloroethyl, propyl, butyl, amyl, hexyl, heptyl, octyl, nonyl, 3,3,5-trimethylhexyl, decyl and lauryl alcohol ; aromatic alkyl alcohols such as phenylcarbinol and methylphenylcarbinol.
  • the blocked polyisocyanates are produced by reacting a sufficient amount of an alcohol with the organic polyisocyanate so that there are no free isocyanate groups.
  • the base coating compositions according to the invention can contain all known pigments or dyes which are customary in the paint industry.
  • Dyes or pigments which can be of an inorganic or organic nature, are, for example, titanium dioxide, graphite, carbon black, zinc chromate, strontrium chromate, barium chromate, lead chromate, lead cyanamide, lead silicochromate, zinc oxide, cadmium sulfide, Chromium oxide, zinc sulfide, nickel titanium yellow, chrome titanium yellow, iron oxide red, iron oxide black, ultramarine blue, phthalocyanine complexes, naphthol red, quinacridones, halogenated thioindigo pigments or the like.
  • metal powders are used individually or in a mixture, such as copper, copper alloys, aluminum and steel, preferably aluminum powder, in at least a predominant proportion, namely in an amount of 0.5 to 25% by weight, based on the total solids content of the coating compositions on binders.
  • metal powders which are specially pretreated for aqueous systems are preferred as metallic pigments.
  • the metal powders can also be used together with one or more of the abovementioned non-metallic pigments or dyes. In this case, their proportion is chosen so that the desired metallic effect is not suppressed.
  • the base coating compositions according to the invention can also contain other customary additives, such as solvents, fillers, plasticizers, stabilizers, wetting agents, dispersing assistants, leveling agents, defoamers and catalysts, individually or in a mixture in the customary amounts. These substances can be added to the individual components and / or the overall mixture.
  • top layer compositions which are not pigmented or only transparent pigmented are suitable as top layer compositions.
  • These can be conventional solvent-borne clearcoats, water-borne clearcoats or powder clearcoats.
  • Pretreated metal substrates are particularly suitable as substrates, but non-pretreated metals and any other substrates such as wood, plastics etc. can also be used. can be coated with a multilayer protective and / or decorative coating using the base coating compositions according to the invention.
  • 255 g of a polyester of 1,6-hexanediol and isophthalic acid with an average molecular weight of 614 are heated to 100 ° C. together with 248 g of a polypropylene glycol with an average molecular weight of 600 and with 100 g of dimethylolpropionic acid Dewatered in a vacuum for 1 hour. 526 g of 4,4'-dicyclohexylmethane diisocyanate and 480 g of methyl ethyl ketone are added at 80 ° C. The mixture is stirred at 80 ° C. until the free isocyanate group content is 1.69%, based on the total weight.
  • the methyl ethyl ketone After adding a mixture of 22.4 g of dimethylethanolamine and 2650 g of deionized water, the methyl ethyl ketone is distilled off in vacuo, and a finely divided dispersion with a solids content of 30%, a pH of 7.4 and a viscosity of 48 s is obtained. measured in a DIN cup.
  • the two-layer coating was produced in accordance with the experimental information given in US Pat. No. 4,558,090.
  • a metallic effect basecoat produced using the polyurethane dispersion according to the invention could be processed into a high-quality two-layer metallic effect coating with an excellent metallic effect.
  • a metal-effect basecoat according to US Pat. No. 4,558,090 and a metal-effect basecoat according to the present invention were applied to a glass plate in a wet film thickness of 100 ⁇ m using a doctor blade.

Abstract

PCT No. PCT/EP86/00736 Sec. 371 Date Aug. 22, 1988 Sec. 102(e) Date Aug. 22, 1988 PCT Filed Dec. 11, 1986 PCT Pub. No. WO87/03829 PCT Pub. Date Jul. 2, 1987.Basecoating compositions for preparing multilayered protective and/or decorative coatings comprise aqueous dispersions which contain (a) as film-forming material one or more polyurethane resins having an acid number of from 5 to 70, which has been prepared by preparing from (A) liner polyetherdiols and/or polyesterdiols having a molecular weight of from 400 to 3,000 (B) diisocyanates and (C) compounds which contain two groups which are reactive toward isocyanate groups, one or more of the compounds used as component C having one or more groups capable of anion formation which have preferably been neutralized before the reaction with a tertiary amine, an intermediate which as terminal isocyanate groups and whose free isocyanate groups have subsequently been reacted with a polyol which contains three or more hydroxyl groups, preferably a triol, (b) pigments and (c) further customary additives.

Description

Die Erfindung betrifft eine Basisbeschichtungszusammen­setzung zur Herstellung von mehrschichtigen, schützenden und/oder dekorativen Überzügen auf Substratoberflächen bestehend aus einer wäßrigen Dispersion, die

  • a) als filmbildendes Material mindestens ein Polyurethan­harz mit einer Säurezahl von 5 bis 70, welches herge­stellt worden ist, indem aus
    (A) linearen Polyether- und/oder Polyesterdiolen mit einem Molekulargewicht von 400 bis 3000
    (B) Diisocyanaten und
    (C) Verbindungen, die zwei gegenüber Isocaynatgruppen reaktive Gruppen enthalten, wobei zumindest ein Teil der als Komponente (C) eingesetzten Ver­bindungen mindestens eine zur Anionenbildung be­fähigte Gruppe aufweist, die vorzugsweise vor der Umsetzung mit einem tertiären Amin neutralisiert worden ist,
    ein endständige Isocyanatgruppen aufweisendes Zwischen­produkt hergestellt worden ist, dessen freie Isocyanat­gruppen anschließend mit
    (D) weiteren, gegenüber Isocyanatgruppen reaktive Gruppen enthaltenden Verbindungen
    umgesetzt worden sind,
  • (b) Pigmente und
  • (c) weitere übliche Additive enthält.
The invention relates to a base coating composition for the production of multilayer, protective and / or decorative coatings on substrate surfaces consisting of an aqueous dispersion, the
  • a) as a film-forming material at least one polyurethane resin with an acid number of 5 to 70, which has been prepared by
    (A) linear polyether and / or polyester diols with a molecular weight of 400 to 3000
    (B) diisocyanates and
    (C) compounds which contain two groups which are reactive toward isocyanate groups, at least some of the compounds used as component (C) having at least one group capable of forming anions which has preferably been neutralized before the reaction with a tertiary amine,
    an intermediate product having terminal isocyanate groups has been prepared, the free isocyanate groups of which are then also present
    (D) further compounds containing groups reactive toward isocyanate groups
    have been implemented
  • (b) pigments and
  • (c) contains other conventional additives.

Insbesondere bei der Automobillackierung aber auch in anderen Bereichen, in denen man Überzüge mit guter dekorativer Wirkung und gleichzeitig einen guten Korrosionsschutz wünscht, ist es bekannt, Substrate mit mehreren, übereinander angeordneten Überzugs­schichten zu versehen.Particularly in automotive painting, but also in other areas in which coatings with a good decorative effect and at the same time good corrosion protection are desired, it is known to provide substrates with a plurality of coating layers arranged one above the other.

Mehrschichtlackierungen werden bevorzugt nach dem sogenannten "Basecoat-Clearcoat"-Verfahren aufge­bracht, d.h. es wird ein pigmentierter Basislack vor­lackiert und nach kurzer Ablüftzeit ohne Einbrennschritt (Naß-in-Naß-Verfahren) mit Klarlack überlackiert. Anschließend werden Basislack und Klarlack zusammen eingebrannt.Multicoat paint systems are preferably applied according to the so-called "basecoat-clearcoat" process, i.e. a pigmented basecoat is pre-coated and after a short flash-off time without a baking step (wet-on-wet process), overcoated with clearcoat. The basecoat and clearcoat are then baked together.

Besonders große Bedeutung hat das "Basecoat-Clearcoat" Verfahren bei der Applikation von Automobil-Metall­effektlacken erlangt.The "basecoat-clearcoat" process has become particularly important in the application of automotive metallic effect paints.

Wirtschaftliche und ökologische Gründe haben dazu geführt, daß versucht wurde, bei der Herstellung von Mehrschichtüberzügen wässrige Basisbeschichtungszu­sammensetzungen einzusetzen.Economic and environmental reasons have led to attempts to use aqueous basecoat compositions in the manufacture of multilayer coatings.

Überzugsmittel zur Herstellung von Basisschichten für mehrschichtige Automobillackierungen müssen nach dem heute üblichen rationellen "Naß-in-Naß"-Verfahren verarbeitbar sein, d.h. sie müssen nach einer möglichst kuzen Vortrockenzeit mit einer (transparenten) Deck­schicht überlackiert werden können, ohne störende Anlöseerscheinungen zu zeigen.Coating agents for the production of base layers for multi-layer automotive coatings must be processable according to the rational "wet-on-wet" process that is customary today, i.e. after a pre-drying time that is as short as possible, it must be possible to overpaint with a (transparent) top coat without showing any annoying signs of dissolving.

Bei der Entwicklung von Überzugsmitteln für Basis­schichten von Metall-Effektlacken müssen außerdem noch weitere Probleme gelöst werden. Der Metalleffekt hängt entscheidend von der Orientierung der Metall-­Pigmentteilchen im Lackfilm ab. Ein im "Naß-in-Naß"-­Verfahren verarbeitbarer Metalleffekt-Basislack muß demnach Lackfilme liefern, in denen die Metall-Pigmente nach der Applikation in einer günstigen räumlichen Orientierung vorliegen und in denen diese Orientierung schnell so fixiert wird, daß sie im Laufe des weiteren Lackierprozesses nicht gestört werden kann.When developing coating compositions for base layers of metal effect paints, further problems also have to be solved. The metal effect depends crucially on the orientation of the metal pigment particles in the paint film. A metal effect basecoat which can be processed in the "wet-on-wet" process must be used accordingly provide paint films in which the metal pigments are in a favorable spatial orientation after application and in which this orientation is quickly fixed in such a way that it cannot be disturbed in the course of the further painting process.

Bei der Entwicklung von wasserverdünnbaren Systemen, die die oben beschriebenen Forderungen erfüllen sollen, treten auf die besonderen physikalischen Eigenschaften des Wassers zurückzuführende, schwer zu lösende Pro­bleme auf und bis heute sind nur wenige wasserver­dünnbare Lacksysteme bekannt, die als Basisbe­schichtungszusammensetzungen im oben dargelegten Sinne verwendet werden können.In the development of water-thinnable systems which are intended to meet the requirements described above, problems that are difficult to solve due to the special physical properties of water arise and to date only a few water-thinnable coating systems are known which can be used as base coating compositions in the sense set out above .

So sind in der US-4,558,090 Überzugsmittel zur Her­stellung der Basisschicht von Mehrschichtüberzügen offenbart, die aus einer wässrigen Dispersion eines Polurethanharzes mit einer Säurezahl von 5 - 70 be­stehen. Die wässrige Polyurethandispersion, die neben dem Bindemittel Pigmente und übliche Zusatzstoffe sowie gegebenenfalls noch weitere Bindemittelkompo­nenten enthalten kann, wird hergestellt durch Umsetzung (A) eines linearen Polyether- und/oder Polyesterdiols mit endständigen Hydroxylgruppen und einem Mole­kulargewicht von 400 bis 3 000, mit
(B) einem Diisocyanat und
(C) einer Verbindung, die zwei gegenüber Isocyanat­gruppen reaktive Gruppen und mindestens eine zur Anionenbildung befähigte Gruppe aufweist, wobei die zur Anionenbildung befähigte Gruppe vor der Umsetzung mit einem tertiären Amin neu­tralisiert worden ist
zu einem Zwischenprodukt mit endständigen Isocyanat­gruppen, Überführung des aus (A), (B) und (C) enthal­tenen Zwischenprodukts in eine überwiegend wäßrige Phase und
(D) Umsetzung der noch vorhandenen Isocyanatgruppen mit einem Di- und/oder Polyamin mit primären und/oder sekundären Aminogruppen.No. 4,558,090, for example, discloses coating compositions for the production of the base layer of multilayer coatings, which consist of an aqueous dispersion of a polyurethane resin with an acid number of 5-70. The aqueous polyurethane dispersion, which in addition to the binder can contain pigments and customary additives and, if appropriate, further binder components, is prepared by reacting (A) a linear polyether and / or polyester diol with terminal hydroxyl groups and a molecular weight of 400 to 3,000
(B) a diisocyanate and
(C) a compound which has two groups reactive toward isocyanate groups and at least one group capable of forming anions, the group capable of forming anions having been neutralized before the reaction with a tertiary amine
to an intermediate product with terminal isocyanate groups, conversion of the intermediate product from (A), (B) and (C) into a predominantly aqueous phase and
(D) reaction of the isocyanate groups still present with a di- and / or polyamine with primary and / or secondary amino groups.

Die in der US 4,558,090 offenbarten Überzugsmittel eignen sich gut zur Herstellung der Basisschicht von Mehrschichtüberzügen, sie sind aber für eine praktische Verwendung vor allem in Serienlackierpro­zessen ungeeignet, weil die schnell trochnenden Über­zugsmittel in den zur Anwendung kommenden Applikations­geräten (z.B. Lackspritzpistole; automatische, elektro­statisch unterstütze Hochrotationsanlagen u.s.w.). so gut haften, daß sie nur unter großen Schwierigkeiten wieder entfernt werden können. Dadurch ist ein vor allem in der Automobilserienlackierung sehr oft schnell durchzuführender Wechsel der applizierten Lacksysteme (z.B. Farbtonwechsel) nicht möglich.The coating agents disclosed in US 4,558,090 are well suited for the production of the base layer of multi-layer coatings, but they are unsuitable for practical use, especially in series painting processes, because the quick drying coating agents in the application devices used (for example paint spray gun; automatic, electrostatically assisted high-speed rotary systems) etc). stick so well that they can only be removed with great difficulty. As a result, it is not possible to change the applied coating systems (e.g. color change) very quickly, especially in automotive serial painting.

Aufgabe der vorliegenden Erfindung war es daher, wässrige Dispersionen zu entwickeln, die als Basis­beschichtungszusammensetzungen zur Herstellung von mehrschichtigen schützenden und/oder dekorativen Überzügen auf Substratoberflächen verwendet werden können und die alle oben dargelegten Forderungen, die an eine Basisbeschichtungszusammensetzung zu stellen sind, erfüllen und auch in den zur Anwendung kommenden Applikationsgeräten problemlos verarbeitet werden können.It was therefore an object of the present invention to develop aqueous dispersions which can be used as base coating compositions for the production of multilayer protective and / or decorative coatings on substrate surfaces and which meet and also meet all the requirements set out above for a base coating composition the application devices used can be processed without any problems.

Diese Aufgabe konnte überraschenderweise durch Ver­wendung von wässrigen Dispersionen gemäß dem Ober­begriff des Anspruchs 1 gelöst werden, die dadurch gekennzeichnet sind, daß das Polyurethanharz durch eine Umsetzung des aus (A) und (B) sowie (C) erhaltenen Zwischenproduktes mit einem mindestens drei Hydroxyl­gruppen enthaltenden Polyol, vorzugsweise Triol, und Überführung des so gewonnenen Reaktionsproduktes in die wässrige Phase hergestellt worden ist.This object was surprisingly achieved by using aqueous dispersions according to the preamble of claim 1, which are characterized in that the polyurethane resin by reacting the intermediate product obtained from (A) and (B) and (C) with an at least three hydroxyl groups Polyol, preferably triol, and transfer of the reaction product thus obtained into the aqueous phase.

Es ist überraschend und war nicht vorhersehbar, daß die auf die ansich gewünschten Eigenschaften (schnelles Antrocknen des aufgebrachten Naßfilms, erschwertes Wiederanlösen des angetrockneten Films) zurückzu­führenden Schwierigkeiten bei der Entfernung von in den Applikationsgeräten zurückgebliebenen Lack­resten durch Verwendung der erfindungsgemäßen wässrigen Polyurethandispersion gelöst werden können und daß keine qualitative Einbußen in der fertiggestellten Mehrschichtlackierung in Kauf genommen werden müssen.It is surprising and was not foreseeable that the difficulties due to the desired properties (quick drying of the applied wet film, difficult re-dissolving of the dried film) in the removal of paint residues remaining in the application devices can be solved by using the aqueous polyurethane dispersion according to the invention and that no loss of quality in the finished multi-layer coating has to be accepted.

Die erfindungsgemäßen Dispersionen werden erhalten, indem die Komponenten (A), (B) und (C) zu einem endständige Isocyanatgruppen aufweisenden Zwischen­produkt umgesetzt werden. Die Umsetzung der Komponenten (A), (B) und (C) erfolgt nach den gut bekannten Ver­fahren der organischen Chemie, wobei bevorzugt eine stufenweise Umsetzung der Komponenten (z.B. Bildung eines ersten Zwischenproduktes aus den Komponenten (A) und (B), das dann mit (C) zu einem zweiten Zwischenprodukt umgesetzt wird) durchgeführt wird. Es ist aber auch eine gleichzeitige Umsetzung der Komponenten (A), (B) und (C) möglich.The dispersions according to the invention are obtained by reacting components (A), (B) and (C) to form an intermediate product containing terminal isocyanate groups. The reaction of components (A), (B) and (C) takes place according to the well-known methods of organic chemistry, preferably a step-by-step reaction of the components (for example formation of a first intermediate product from components (A) and (B), the is then reacted with (C) to form a second intermediate). However, components (A), (B) and (C) can also be reacted simultaneously.

Die Umsetzung wird bevorzugt in Lösungsmitteln durch­geführt, die gegenüber Isocyanatgruppen inert und mit Wasser mischbar sind. Vorteilhaft werden Lösungs­mittel eingesetzt, die neben den oben beschriebenen Eigenschaften auch noch gute Löser für die hergestellten Polyurethane sind sich aus wässrigen Mischungen leicht abtrennen lassen. Besonders gut geeignete Lösungsmittel sind Aceton und Methylethylketon.The reaction is preferably carried out in solvents which are inert to isocyanate groups and are miscible with water. Solvents are advantageously used which, in addition to the properties described above, are also good solvents for the polyurethanes produced and can be easily separated from aqueous mixtures. Acetone and methyl ethyl ketone are particularly suitable solvents.

Als Komponente (A) können prinzipiell alle bei der Herstellung von Beschichtungsmitteln auf Polyurethan­basis gebräuchlichen Diole eingesetzt werden. Geeig­nete Polyetherdiole entsprechen der allgemeinen For­mel:

Figure imgb0001
in der R = Wasserstoff oder ein niedriger Alkylrest, gegebenenfalls mit verschiedenen Substituenten, ist, n = 2 bis 6 und m = 10 bis 50 oder noch höher ist. Beispiele sind Poly(oxytetramethylen)glykole, Poly(oxyethylen)glykole und Poly(oxypropylen)glykole.In principle, all diols customary in the production of coating compositions based on polyurethane can be used as component (A). Suitable polyether diols correspond to the general formula:
Figure imgb0001
in which R = hydrogen or a lower alkyl radical, optionally with different substituents, n = 2 to 6 and m = 10 to 50 or even higher. Examples are poly (oxytetramethylene) glycols, poly (oxyethylene) glycols and poly (oxypropylene) glycols.

Die bevorzugten Polyalkylenetherpolyole sind Poly­(oxypropylen)glykole mit einem Molekulargewicht im Bereich von 400 bis 3 000.The preferred polyalkylene ether polyols are poly (oxypropylene) glycols with a molecular weight in the range of 400 to 3,000.

Polyesterdiole können ebenfalls als polymere Diol­komponente (Komponente A) bei der Erfindung verwendet werden. Man kann die Polyesterdiole durch Veresterung von organischen Dicarbonsäuren oder ihren Anhydriden mit organischen Diolen herstellen. Die Dicarbonsäuren und die Diole können aliphatische oder aromatische Dicarbonsäuren und Diole sein.Polyester diols can also be used as the polymeric diol component (component A) in the invention. The polyester diols can be prepared by esterifying organic dicarboxylic acids or their anhydrides with organic diols. The dicarboxylic acids and the diols can be aliphatic or aromatic dicarboxylic acids and diols.

Die zur Herstellung der Polyester verwendeten Diole schließen Alkylenglykole wie Ethylenglykol, Butylen­glykol, Neopentyglykol und andere Glykole wie Di­methylolcyclohexan ein.The diols used to make the polyesters include alkylene glycols such as ethylene glycol, butylene glycol, neopenty glycol and other glycols such as dimethylolcyclohexane.

Die Säurekomponente des Polyesters besteht in erster Linie aus niedermolekularen Dicarbonsäuren oder ihren Anhydriden mit 2 bis 18 Kohlenstoffatomen im Molekül.The acid component of the polyester consists primarily of low molecular weight dicarboxylic acids or their anhydrides with 2 to 18 carbon atoms in the molecule.

Geeignete Säuren sind beispielsweise Phtalsäure, Isophthalsäure, Terephthalsäure, Tetrahydrophthal­säure, Hexahydrophthalsäure, Adipinsäue, Azelainsäure, Sebazinsäure, Maleinsäure, Glutarsäure, Hexachlor­heptandicarbonsäure und Tetrachlorphthalsäure. Anstelle dieser Säuren können auch ihre Anhydride, soweit diese existieren, verwendet werden.Suitable acids are, for example, phthalic acid, isophthalic acid, terephthalic acid, tetrahydrophthalic acid, hexahydrophthalic acid, adipic acids, azelaic acid, sebacic acid, maleic acid, glutaric acid, hexachlorheptanedicarboxylic acid and tetrachlorophthalic acid. Instead of these acids, their anhydrides can also be used these exist.

Ferner lassen sich bei der Erfindung auch Polyester­diole, die sich von Lactonen ableiten, als Komponente (A) benutzen. Diese Produkte erhält man beispielsweise durch die Umsetzung eines ε-Caprolactons mit einem Diol. Solche Produkte sind in der US-PS 3 169 945 beschrieben.In addition, polyester diols derived from lactones can also be used as component (A) in the invention. These products are obtained, for example, by reacting an ε-caprolactone with a diol. Such products are described in U.S. Patent 3,169,945.

Die Polylactonpolyole, die man durch diese Umsetzung erhält, zeichnen sich durch die Gegenwart einer end­ständigen Hydroxylgruppe und durch wiederkehrende Polyesteranteile, die sich von dem Lacton ableiten, aus. Diese wiederkehrenden Molekülanteile können der Formel
-

Figure imgb0002
- (CHR)n - CH₂O -
entsprechen, in der n bevorzugt 4 bis 6 ist und der Substituent Wasserstoff, ein Alkylrest, ein Cyclo­alkylrest oder ein Alkoxyrest ist, wobei kein Sub­stituent mehr als 12 Kohlenstoffatome enthält und die gesamte Anzahl der Kohlenstoffatome in dem Sub­stituenten in dem Lactonring 12 nicht übersteigt.The polylactone polyols which are obtained by this reaction are distinguished by the presence of a terminal hydroxyl group and by recurring polyester fractions which are derived from the lactone. These recurring molecular parts can be of the formula
-
Figure imgb0002
- (CHR) n - CH₂O -
in which n is preferably 4 to 6 and the substituent is hydrogen, an alkyl radical, a cycloalkyl radical or an alkoxy radical, where no substituent contains more than 12 carbon atoms and the total number of carbon atoms in the substituent in the lactone ring does not exceed 12.

Das als Ausgangsmaterial verwendete Lacton kann ein beliebiges Lacton oder eine beliebige Kombination von Lactonen sein, wobei dieses Lacton mindestens 6 Kohlenstoffatome in dem Ring enthalten sollte, zum Beispiel 6 bis 8 Kohlenstoffatome und wobei min­destens 2 Wasserstoffsubstituenten an dem Kohlenstoff­atom vorhanden sein solten, das an die Sauerstoff­gruppe des Rings gebunden ist. Das als Ausgangsmaterial verwendete Lacton kann durch die folgende allgemeine Formel dargestellt werden.

Figure imgb0003
in den n und R die bereits angegebene Bedeutung haben.The lactone used as the starting material can be any lactone or any combination of lactones, which lactone should contain at least 6 carbon atoms in the ring, for example 6 to 8 carbon atoms and where there should be at least 2 hydrogen substituents on the carbon atom attached to the Oxygen group of the ring is bound. The lactone used as a raw material can be represented by the following general formula.
Figure imgb0003
 in the n and R have the meaning already given.

Die bei der Erfindung für die Herstellung der Poly­esterdiole bevorzugten Lactone sind die Caprolac­tone, bei denen n den Wert 4 hat. Das am meisten bevorzugte Lacton ist das unsubstituierte ε-Capro­lacton, bei dem n den Wert 4 hat und alle R-Substituen­ten Wasserstoff sind. Dieses Lacton wird besonders bevorzugt, da es in großen Mengen zur Verfügung steht und Überzüge mit ausgezeichneten Eigenschaften ergibt. Außerdem können verschiedene andere Lactone einzeln oder in Kombination benutzt werden.The lactones preferred for the preparation of the polyester diols in the invention are the caprolactones, in which n has the value 4. The most preferred lactone is the unsubstituted ε-caprolactone, where n is 4 and all R substituents are hydrogen. This lactone is particularly preferred because it is available in large quantities and gives coatings with excellent properties. In addition, various other lactones can be used individually or in combination.

Beispiele von für die Umsetzung mit dem Lacton geeig­neten aliphatischen Diolen schließen ein Ethylen­glykol, 1,3-Propandiol, 1,4-Butandiol, Dimethylol­cyclohexan.Examples of aliphatic diols suitable for reaction with the lactone include ethylene glycol, 1,3-propanediol, 1,4-butanediol, dimethylolcyclohexane.

Als Komponente (B) können für die Herstellung der Polyurethandispersion beliebige organische Diisocyanate eingesetzt werden. Beispiele von geeigneten Diiso­cyanaten sind Trimethylendiisocyanat, Tetramethylen­diisocyanat, Pentamethylendiisocyanat, Hexamethylen­diisocyanat, Propylendiisocyanat, Ethylethylen­diisocyanat , 2,3-Dimethylethylendiisocyanat, 1-Methyl­trimethylendiisocyanat, 1,3-Cyclopentylendiisocyanat, 1,4-Cyclohexylendiisocyanat, 1,2-Cyclohexylendiisocya­nat, 1,3-Phelendiisocyanat, 1,4-Phenylendiisocyanat, 2,4-Toluylendiisocyanat, 2,6-Toluylendiisocyanat, 4,4ʹ-­Biphenylendiisocyanat, 1,5-Naphthylendiisocyanat, 1,4-Naphthylendiisocyanat, 1-Isocyanatomethyl-5-isocya­nato-1,3,3-trimethylcyclohexan, Bis-(4-isocyanatocyclo­hexyl)methan, Bis-(4-isocyanatophenyl)-methan, 4,4ʹ-­Diisocyanatodiphenylether und 2,3-Bis-(8-isocyanato­octyl)-4-octyl-5-hexyl-cyclohexen.Any organic diisocyanates can be used as component (B) for the production of the polyurethane dispersion. Examples of suitable diisocyanates are trimethylene diisocyanate, tetramethylene diisocyanate, pentamethylene diisocyanate, hexamethylene diisocyanate, propylene diisocyanate, ethyl ethylene diisocyanate, 2,3-dimethylethylene diisocyanate, 1-methyltrimethylene diisocyanate, 1,3-cyclopentylene diisocyanate, 1,4-cyclohexylene diisocyanate diisocyanate, 1,2-diisocyanate diisocyanate, 1,2-diisocyanate diisocyanate, 1,2-cyclohexylene diisocyanate, 1,2-diisocyanate diisocyanate, 1,2-cyclohexylene diisocyanate, 1,2-diisocyanate, 1,2-diisocyanate, 1,2-diisocyanate, 1,2-diisocyanate and 1,2-diisocyanate , 1,4-phenylene diisocyanate, 2,4-tolylene diisocyanate, 2,6-tolylene diisocyanate, 4,4'-biphenylene diisocyanate, 1,5-naphthylene diisocyanate, 1,4-naphthylene diisocyanate, 1-isocyanatomethyl-5-isocyanato-1,3,3 trimethylcyclohexane, bis (4-isocyanatocyclohexyl) methane, bis (4-isocyanatophenyl) methane, 4,4'-diisocyanatodiphenyl ether and 2,3-bis (8-isocyanato-octyl) -4-octyl-5-hexyl-cyclohexene.

Als Komponente (C) werden Verbindungen eingesetzt, die zwei gegenüber Isocyanatgruppen reaktive Gruppen enthalten, wobei zumindest ein Teil der als Komponente (C) eingesetzten Verbindungen mindestens eine zur Anionenbildung befähigte Gruppe aufweist, die vorzugs­weise vor der Umsetzung mit einem tertiären Amin neutralisiert worden ist.Compounds which contain two groups which are reactive toward isocyanate groups are used as component (C), at least some of which are used as components (C) compounds used has at least one group capable of forming anions, which has preferably been neutralized before the reaction with a tertiary amine.

Durch Einstellung eines bestimmten Mischungsver­hältnisses zwischen den zur Anionenbildung befähigten Gruppen enthaltenden und den von diesen Gruppen freien Verbindungen kann der Anteil an ionischen Gruppen im Polyurethanmolekül gesteuert werden.The proportion of ionic groups in the polyurethane molecule can be controlled by setting a certain mixing ratio between the groups containing the groups capable of forming anions and the compounds free of these groups.

Geeignete mit Isocyanatgruppen reagierende Gruppen sind insbesondere Hydroxylgruppen. Die Verwendung von Verbindungen, die primäre oder sekundäre Amino­gruppen enthalten, kann einen negativen Einfluß auf die oben beschriebene Verarbeitbarkeit der Dispersionen haben. Art und Menge von gegebenenfalls einzusetzenden aminogruppenhaltigen Verbindungen sind vom Durch­schnittsfachmann durch einfach durchzuführende Routine­untersuchungen zu ermitteln.Suitable groups reacting with isocyanate groups are in particular hydroxyl groups. The use of compounds containing primary or secondary amino groups can have a negative impact on the processability of the dispersions described above. The type and amount of any compounds containing amino groups to be used can be determined by the person skilled in the art by means of routine tests which are simple to carry out.

Als zur Anionenbildung befähigte Gruppen kommen vor allem Carboxyl- und Sulfonsäuregruppen in Betracht. Diese Gruppen können vor der Umsetzung mit einem tertiären Amin neutralisiert werden, um eine Reaktion mit den Isocyanatgruppen zu vermeiden.Carboxyl and sulfonic acid groups are particularly suitable as groups capable of forming anions. These groups can be neutralized with a tertiary amine before the reaction in order to avoid reaction with the isocyanate groups.

Als Verbindung, die mindestens zwei mit Isocyanat­gruppen reagierende Gruppen und mindestens eine zur Anionenbildung befähigte Gruppe enthält, sind beispiels­weise Dihydroxypropionsäure Dimethylolpropionsäure, Dihydroxybernsteinsäure oder Dihydroxybenzoesäure geeignet. Geeignet sind auch die durch Oxydation von Monosacchariden zugänglichen Polyhydroxysäuren, z.B. Glukonsäure, Zuckersäure, Schleimsäure, Glukuronsäure und dergleichen.
Aminogruppenhaltige Verbindungen sind beispielsweise α,δ-Diaminovaleriansäure, 3,4-Diaminobenzoesäure, 2,4-Diamino-toluol-sulfonsäure-(5), 4,4ʹ-Diamino-di­phenylethersulfonsäure und dergleichen.Dihydroxypropionic acid, dimethylolpropionic acid, dihydroxysuccinic acid or dihydroxybenzoic acid, for example, are suitable as the compound which contains at least two groups reacting with isocyanate groups and at least one group capable of forming anions. Also suitable are the polyhydroxy acids obtainable by oxidation of monosaccharides, for example gluconic acid, sugar acid, mucic acid, glucuronic acid and the like.
Compounds containing amino groups are, for example, α, δ-diaminovaleric acid, 3,4-diaminobenzoic acid, 2,4-diamino-toluenesulfonic acid- (5), 4,4'-diamino-diphenyl ether sulfonic acid and the like.

Geeignete tertiäre Amine zur Neutralisation der anionischen Gruppen sind beispielsweise Trimethylamin Triethylamin, Dimethylanilin, Diethylanilin, Tri­phenylamin und dergleichen.Suitable tertiary amines for neutralizing the anionic groups are, for example, trimethylamine, triethylamine, dimethylaniline, diethylaniline, triphenylamine and the like.

Als Verbindungen, die zwei gegenüber Isocyanatgruppen reaktive Gruppen aufweisen, jedoch frei von zur Anionen­bildung befähigten Gruppen sind, können beispielsweise niedermolekulare Diole oder Diamine mit primären oder sekundären Aminogruppen eingesetzt werden.Low molecular weight diols or diamines with primary or secondary amino groups can be used, for example, as compounds which have two groups reactive toward isocyanate groups but are free from groups capable of forming anions.

Das aus (A), (B) und (C) gebildete isocyanatgruppen­haltige Zwischenprodukt wird mit dem mindestens drei Hydroxylgruppen enthaltenden Polyol umgesetzt, was höchstwahrscheinlich eine Kettenverlängerung und gegebenenfalls auch eine Verzweigung des Bindemittel­moleküls zur Folge hat.The isocyanate group-containing intermediate formed from (A), (B) and (C) is reacted with the polyol containing at least three hydroxyl groups, which most likely results in chain extension and possibly also branching of the binder molecule.

Bei dieser Umsetzung muß sorgfältig darauf geachtet werden, daß keine vernetzten Produkte erhalten werden.During this implementation, care must be taken to ensure that no cross-linked products are obtained.

Das kann zum Beispiel durch Zugabe einer auf den Isocyanatgruppengehalt des aus (A), (B) und (C) erhal­tenen Zwischenproduktes und die Reaktionsbedingungen abgestimmten Menge an Polyol erreicht werden.This can be achieved, for example, by adding an amount of polyol matched to the isocyanate group content of the intermediate product obtained from (A), (B) and (C) and the reaction conditions.

Im Prinzip sind alle mindestens drei Hydroxylgruppen enthaltenden Polyole, die mit dem aus (A), (B) und (C) erhaltenen Zwischenprodukt so umgesetzt werden können, daß keine vernetzten Produkte entstehen, zur Herstellung der erfindungsgemäßen Polyurethandispersion geeignet. Als Beispiele seien Trimethylolpropan, Glycerin, Erythrit, Mesoerythrit, Arabit, Adonit, Xylit, Mannit, Sorbit, Dulcit, Hexantriol, (Poly)-­Pentaerythritol u.s.w. genannt.In principle, all polyols containing at least three hydroxyl groups, which can be reacted with the intermediate product obtained from (A), (B) and (C) in such a way that no crosslinked products are formed, are suitable for producing the polyurethane dispersion according to the invention. Examples include trimethylolpropane, glycerol, erythritol, mesoerythritol, arabitol, adonitol, xylitol, mannitol, sorbitol, dulcitol, hexanetriol, (poly) -pentaerythritol, etc.

Ganz besonders gute Ergebnisse können erzielt werden, wenn Trimethylolpropan als Polyol eingesetzt wird.Particularly good results can be achieved if trimethylolpropane is used as the polyol.

Es ist auch denkbar, daß durch gleichzeitige Umsetzung aller vier Komponenten (A), (B), (C) und Polyol unvernetzte Polyurethane herstellbar sind, die zu brauchbaren Basisbeschichtungszusammensetzungen verarbeitet werden können.It is also conceivable that by simultaneously reacting all four components (A), (B), (C) and polyol, uncrosslinked polyurethanes can be produced which can be processed to useful base coating compositions.

Nach der Umsetzung des aus (A), (B) und (C) erhaltenen Zwischenproduktes mit der Polyolkomponente, die vor­zugsweise in einem gegenüber Isocyanatgruppen inerten, mit Wasser mischbaren, das entstehende Polyurethan gut lösenden und aus wässrigen Mischungen gut abtrenn­baren Lösungsmitteln (z.B. Aceton oder Methylethyl - keton) durchgeführt worden ist und gegebenenfalls noch durchzuführenden Neutralisierung der zur Anionen­bildung befähigten Gruppen wird das Reaktionsprodukt in eine wässrige Phase überführt. Das kann zum Beispiel durch Dispergierung des Reaktionsgemisches in Wasser und Abdestillieren der unter 100 °C siedenden orga­nischen Lösungsmittelanteile geschehen.After the reaction of the intermediate product obtained from (A), (B) and (C) with the polyol component, which is preferably in a solvent which is inert to isocyanate groups and which is miscible with water, the resulting polyurethane dissolves well and can easily be separated from aqueous mixtures (e.g. acetone or Methyl ethyl ketone) has been carried out and, if necessary, neutralization of the groups capable of forming anions is carried out, the reaction product is converted into an aqueous phase. This can be done, for example, by dispersing the reaction mixture in water and distilling off the organic solvent components boiling below 100 ° C.

Unter wässriger Phase ist Wasser, das auch noch orga­nische Lösungsmittel enthalten kann, zu verstehen. Als Beispiele für Lösungemittel, die im Wasser vor­handen sein können, seien heterocyklische, aliphatische oder aromatische Kohlenwasserstoffe, ein- oder mehrwer­tige Alkohole, Ether, Ester und Ketone, wie zum Bei­spiel N-Methylpyrrolidon, Toluol, Xylol, Butanol, Ethyl- und Butylglykol sowie deren Acetate, Butyl­diglycol, Ethylenglykoldibutylether, Ethylenglykoldi­ethylether, Diethylenglykoldimethylether, Cyclohexanon, Methylethylketon, Aceton, Isophoron oder Mischungen davon genannt.The aqueous phase is understood to mean water, which can also contain organic solvents. Examples of solvents which may be present in water are heterocyclic, aliphatic or aromatic hydrocarbons, mono- or polyhydric alcohols, ethers, esters and ketones, such as, for example, N-methylpyrrolidone, toluene, xylene, butanol, ethyl and butyl glycol and their acetates, butyl diglycol, ethylene glycol dibutyl ether, ethylene glycol diethyl ether, diethylene glycol dimethyl ether, cyclohexanone, methyl ethyl ketone, acetone, isophorone or mixtures thereof.

Nachdem der pH-Wert der resultierenden Polyurethan­dispersion kontrolliert und gegebenenfalls auf einen Wert zwischen 6 und 9 eingestellt worden ist, bildet die Dispersion die Grundlage der erfindungsgemäßen Überzugsmittel, in die die übrigen Bestandteile wie z.B. zusätzliche Bindemittel, Pigmente, organische Lösungsmittel und Hilfsstoffe durch Dispergieren bei­spielsweise mittels eines Rührers oder Dissolvers homogen eingearbeitet werden. Abschließend wird erneut der pH-Wert kontrolliert und gegebenenfalls auf einen Wert von 6 bis 9, vorzugsweise 7,0 bis 8,5 eingesetellt. Weiterhin werden der Festkörpergehalt und die Viskosi­tät auf die an die jeweiligen Applikationsbedingungen angepaßten Werte eingestellt.After the pH of the resulting polyurethane dispersion has been checked and, if necessary, adjusted to a value between 6 and 9, the dispersion forms the basis of the coating compositions according to the invention, into which the other constituents, such as e.g. Additional binders, pigments, organic solvents and auxiliaries can be incorporated homogeneously by dispersing, for example using a stirrer or dissolver. Finally, the pH is checked again and, if necessary, adjusted to a value of 6 to 9, preferably 7.0 to 8.5. Furthermore, the solids content and the viscosity are adjusted to the values adapted to the respective application conditions.

Die gebrauchsfertigen Überzugsmittel weisen in der Regel einen Festkörperanteil von 10 bis 30 Gew.-% auf, und ihre Auslaufzeit im ISO-Becher 4 beträgt 15 bis 30 Sekunden, vorzugsweise 18 bis 25 Sekunden. Ihr Anteil an Wasser beträgt 60 bis 90 Gew.-%, der an organischen Lösungsmitteln 0 bis 20 Gew.-%, jeweils bezogen auf das gesamte Überzugsmittel.The ready-to-use coating compositions generally have a solids content of 10 to 30% by weight and their run-out time in the ISO cup 4 is 15 to 30 seconds, preferably 18 to 25 seconds. Their proportion of water is 60 to 90% by weight, that of organic solvents 0 to 20% by weight, in each case based on the total coating agent.

Die vorteilhaften Wirkungen der erfindungsgemäßen Beschichtungszusammensetzungen sind auf den Einsatz der oben beschriebenen wässrigen Polyurethandispersion zurückzuführen.The advantageous effects of the coating compositions according to the invention can be attributed to the use of the aqueous polyurethane dispersion described above.

In vielen Fällen ist es wünschenswert, die Eigenschaften der erhaltenen Überzüge durch Mitverwendung weiterer Bindemittelsysteme in der Basis-Beschichtungszusammen­setzung gezielt zu verbessern.In many cases it is desirable to specifically improve the properties of the coatings obtained by using additional binder systems in the base coating composition.

Die erfindungsgemäßen Basis-Beschichtungszusammen­setzungen enthalten vorteilhaft als zusätzliche Binde­mittelkomponente ein wasserverdünnbares Melaminharz in einem Anteil von 1 bis 80 Gew.-%, bevorzugt 20 bis 60 Gew.-%, bezogen auf den Festkörpergehalt der Polyurethandispersion.The base coating compositions according to the invention advantageously contain, as an additional binder component, a water-dilutable melamine resin in a proportion of 1 to 80% by weight, preferably 20 to 60% by weight, based on the solids content of the polyurethane dispersion.

Wasserlösliche Melaminharze sind an sich bekannt und werden in größerem Umfang eingesetzt. Es handelt sich hierbei um veretherte Melamin-Formaldehyd-Konden­sationsprodukte. Ihre Wasserlöslichkeit hängt abgesehen vom Kondensationsgrad, der möglichst niedrig sein soll, von der Veretherungskomponente ab, wobei nur die niedrigsten Glieder der Alkanol- bzw. Ethylenglykol­monoetherreihe wasserlösliche Kondensate ergeben. Die größte Bedeutung haben die Hexamethoxymethylmelamin­harze. Bei Verwendung von Lösungsvermittlern können auch butanolveretherte Melaminharze in wäßriger Phase dispergiert werden.Water-soluble melamine resins are known per se and are used on a larger scale. These are etherified melamine-formaldehyde condensation products. Apart from the degree of condensation, which should be as low as possible, their solubility in water depends on the etherification component, only the lowest members of the alkanol or ethylene glycol monoether series giving water-soluble condensates. Hexamethoxymethylmelamine resins are of the greatest importance. If solubilizers are used, butanol-etherified melamine resins can also be dispersed in the aqueous phase.

Es besteht auch die Möglichkeit, Carboxylgruppen in das Kondensat einzufügen. Umetherungsprodukte hoch­veretherter Formaldehydkondensate mit Oxycarbonsäuren sind über ihre Carboxylgruppe nach Neutralisation wasserlöslich und könne als Vernetzerkomponente in den erfindungsgemäßen Überzugsmitteln eingesetzt werden.It is also possible to insert carboxyl groups in the condensate. Transetherification products of highly etherified formaldehyde condensates with oxycarboxylic acids are water-soluble via their carboxyl group after neutralization and can be used as a crosslinking component in the coating compositions according to the invention.

Anstelle der beschriebenen Melaminharze können auch andere wasserlösliche oder wasserdispergierbare Amino­harze wie z.B. Benzoguanaminharze eingesetzt werden.Instead of the melamine resins described, other water-soluble or water-dispersible amino resins such as e.g. Benzoguanamine resins are used.

Für den Fall, daß die erfindungsgemäße Basisbe­schichtungszusammensetzung ein Melaminharz enthält, kann sie vorteilhaft zusätzlich als weitere Bindemittel­komponente ein wasserverdünnbares Polyesterharz und/oder ein wasserverdünnbares Polyacrylatharz enthalten, wobei das Gewichtsverhältnis Melaminharz : Polyester-/Poly­acrylatharz 2:1 bis 1:4 beträgt und der Gesamtanteil an Melaminharz, Polyester-/Polyacrylatharz, bezogen auf den Festkörpergehalt der Polyurethandispersion 1 bis 80 Gew.-%, bevorzugt 20 bis 60 Gew.-% beträgt.In the event that the base coating composition according to the invention contains a melamine resin, it can advantageously additionally contain, as a further binder component, a water-dilutable polyester resin and / or a water-dilutable polyacrylate resin, the weight ratio of melamine resin: polyester / polyacrylate resin being 2: 1 to 1: 4 and the total proportion of melamine resin, polyester / polyacrylate resin, based on the solids content of the polyurethane dispersion, is 1 to 80% by weight, preferably 20 to 60% by weight.

Wasserverdünnbare Polyester sind solche mit freien Carboxylgruppen, d.h. Polyester mit hoher Säurezahl.Water-dilutable polyesters are those with free carboxyl groups, ie polyesters with a high acid number.

Es sind grundsätzlich zwei Methoden bekannt, die be­nötigten Carboxylgruppen in das Harzsystem einzufügen. Der erste Weg besteht darin, die Veresterung bei der gewünschten Säurezahl abzubrechen. Nach Neutralisation mit Basen sind die so erhaltenen Polyester in Wasser löslich und verfilmen beim Einbrennen. Die zweite Mög­lichkeit besteht in der Bildung partieller Ester von Di- oder Polycarbonsäuren mit hydroxylreichen Polyestern mit niedriger Säurezahl. Für diese Reaktion werden überlicherweise Anhydride der Dicarbonsäuren herange­zogen, welche unter milden Bedingungen unter Ausbildung einer freien Carboxylgruppe mit der Hydroxylkomponente umgesetzt werden.There are basically two methods known for inserting the required carboxyl groups into the resin system. The first way is to terminate the esterification at the desired acid number. After neutralization with bases, the polyesters thus obtained are soluble in water and form a film when baked. The second possibility is the formation of partial esters of di- or polycarboxylic acids with hydroxyl-rich polyesters with a low acid number. For this reaction, anhydrides of dicarboxylic acids are usually used, which are reacted with the hydroxyl component under mild conditions to form a free carboxyl group.

Die wasserverdünnbaren Polyacrylatharze enthalten ebenso wie die oben beschriebenen Polyesterharze freie Carboxylgruppen. Es handelt sich in der Regel um Acryl- bzw. Methacrylcopolymerisate, und die Carboxylgruppen stammen aus den Anteilen an Acryl- oder Methacrylsäure.Like the polyester resins described above, the water-dilutable polyacrylate resins contain free carboxyl groups. They are usually acrylic or methacrylic copolymers, and the carboxyl groups come from the proportions of acrylic or methacrylic acid.

Als Vernetzungsmittel können auch blockierte Poly­isocyanate eingesetzt werden. Es können bei der Er­findung beliebige Polyisocyanate benutzt werden, bei denen die Isocyanatgruppen mit einer Verbindung umge­setzt worden sind, so daß das gebildete blockierte Polyisocyanat gegenüber Hydroxylgruppen bei Raumtem­peraturen beständig ist, bei erhöhten Temperaturen, in der Regel im Bereich von etwa 90 bis 300 °C, aber reagiert. Bei der Herstellung der blockierten Polyiso­cyanate können beliebige für die Vernetzung geeignete organische Polyisocyanate verwendet werden. Bevorzugt sind die Isocyanate, die etwa 3 bis etwa 36, insbe­sondere etwa 8 bis 15 Kohlenstoffatome enthalten. Bei­spiele von geeigneten Diisocyanaten sind die oben genannten Diisocyanate (Komponente B).
Es können auch Polyisocyanate von höherer Isocyanat­funktionalität verwendet werden. Beispiele dafür sind Tris-(4-isocyanatophenyl)-methan, 1,3,5-Triisocyanato­benzol, 2,4,6-Triisocyanatotoluol, 1,3,5-Tris-(6-iso­ cyanatohexyl)-biuret. Bis-(2,5-diisocyanato-4-methyl­phenyl)-methan und polymere Polyisocyanate, wie Dimere und Trimere von Diisocyanatotoluol. Ferner kann man auch Mischungen von Polyisocyanaten benutzen..Blocked polyisocyanates can also be used as crosslinking agents. Any polyisocyanates in which the isocyanate groups have been reacted with a compound can be used in the invention, so that the blocked polyisocyanate formed is resistant to hydroxyl groups at room temperature, at elevated temperatures, generally in the range from about 90 to 300 ° C. , but responds. Any organic polyisocyanates suitable for crosslinking can be used in the preparation of the blocked polyisocyanates. The isocyanates which contain about 3 to about 36, in particular about 8 to 15, carbon atoms are preferred. Examples of suitable diisocyanates are the above-mentioned diisocyanates (component B).
Polyisocyanates with higher isocyanate functionality can also be used. Examples include tris (4-isocyanatophenyl) methane, 1,3,5-triisocyanatobenzene, 2,4,6-triisocyanatotoluene, 1,3,5-tris (6-iso cyanatohexyl) biuret. Bis (2,5-diisocyanato-4-methylphenyl) methane and polymeric polyisocyanates such as dimers and trimers of diisocyanatotoluene. Mixtures of polyisocyanates can also be used.

Die bei der Erfindung als Vernetzungsmittel in Betracht kommenden organischen Polyisocyanate können auch Prä­polymere sein, die sich beispielsweise von einem Polyol einschließlich eines Polyetherpolyols oder eines Poly­esterpolyols ableiten. Dazu werden bekanntlich Polyole mit einem Überschuß von Polyisocyanaten umgesetzt, wodurch Präpolymere mit endständigen Isocyanatgruppen entstehen. Beispiele von Polyolen, die hierfür verwendet werden können, sind einfache Polyole, wie Glykole, z.B. Ethylenglykol und Propylenglykol, und andere Polyole, wie Glycerin, Trimethylolpropan, Hexantriol und Pentaerythrit; ferner Monoether, wie Diethylen­glykol und Dipropylenglykol sowie Polyether, die Addukte aus solchen Polyolen und Alkylenoxiden sind. Beispiele von Alkylenoxiden, die sich für eine Poly­addition an diese Polyole unter Bildung von Polyethern eignen, sind Ethylenoxid, Propylenoxid, Butylenoxid und Styroloxid. Man bezeichnet diese Polyadditionspro­dukte im allgemeinen als Polyether mit endständigen Hydroxylgruppen. Sie können linear oder verzweigt sein. Beispiele von solchen Polyethern sind Polyoxyethylen­glykol von einem Molekulargewicht von 1 540, Poly­oxypropylenglykol mit einem Molekulargewicht von 1 025, Polyoxytetramethylenglykol, Polyoxyhexamethylen­glykol, Polyoxynonamethylenglykol, Polyoxydecamethylen­glykol, Polyoxydodecamethylenglykol und Mischungen davon. Andere Typen von Polyoxyalkylenglykolethern können ebenfalls verwendet werden. Besonders geeignete Polyetherpolyole sind diejenigen, die man erhält durch Umsetzung von derartigen Polyolen, wie Ethylen­glykol, Diethylenglykol, Triethylenglykol, 1,4-­Butandiol, 1,3-Butandiol, 1,6-Hexandiol und Mischungen davon; Glycerintrimethylolethan, Trimethylolpropan, 1,2,6-Hexantriol, Dipentaerythrit, Tripentaerythrit, Polypentaerythrit, Methylglukosiden und Saccharose mit Alkylenoxiden, wie Ethylenoxid, Propylenoxid oder Mischungen davon.The organic polyisocyanates which are suitable as crosslinking agents in the invention can also be prepolymers which are derived, for example, from a polyol, including a polyether polyol or a polyester polyol. For this purpose, it is known that polyols are reacted with an excess of polyisocyanates, resulting in prepolymers with terminal isocyanate groups. Examples of polyols that can be used for this are simple polyols, such as glycols, for example ethylene glycol and propylene glycol, and other polyols, such as glycerol, trimethylolpropane, hexanetriol and pentaerythritol; also monoethers, such as diethylene glycol and dipropylene glycol, and polyethers, which are adducts of such polyols and alkylene oxides. Examples of alkylene oxides which are suitable for polyaddition to these polyols to form polyethers are ethylene oxide, propylene oxide, butylene oxide and styrene oxide. These polyadducts are generally referred to as polyethers with terminal hydroxyl groups. They can be linear or branched. Examples of such polyethers are polyoxyethylene glycol with a molecular weight of 1,540, polyoxypropylene glycol with a molecular weight of 1,025, polyoxytetramethylene glycol, polyoxyhexamethylene glycol, polyoxynonamethylene glycol, polyoxydecamethylene glycol, polyoxydodecamethylene glycol and mixtures thereof. Other types of polyoxyalkylene glycol ethers can also be used. Particularly suitable polyether polyols are those which are obtained by reacting such polyols, such as ethylene glycol, diethylene glycol, triethylene glycol, 1,4-butanediol, 1,3-butanediol, 1,6-hexanediol and mixtures thereof; Glycerol trimethylol ethane, trimethylol propane, 1,2,6-hexanetriol, dipentaerythritol, tripentaerythritol, polypentaerythritol, methyl glucosides and sucrose with alkylene oxides, such as ethylene oxide, propylene oxide or mixtures thereof.

Für die Blockierung der Polyisocyanate können beliebige geeignete aliphatische, cycloaliphatische oder aroma­tische Alkylmonoalkohole verwendet werden. Beispiele dafür sind aliphatische Alkohole, wie Methyl-, Ethyl-, Chlorethyl-, Propyl-, Butyl-, Amyl-, Hexyl-, Heptyl-, Octyl-, Nonyl-, 3,3,5-Trimethylhexyl-, Decyl- und Laurylalkohol; aromatische Alkylalkohole, wie Phenylcar­binol und Methylphenylcarbinol. Es können auch geringe Anteile an höhermolekularen und relativ schwer flüchti­en Monoalkoholen gegebenenfalls mitverwendet werden, wobei diese Alkohole nach ihrer Abspaltung als Weich­macher in den Überzügen wirken.
Andere geeignete Blockierungsmittel sind Oxime, wie Methylethylketonoxim, Acetonoxim und Cyclohexanon­oxim, sowie auch Caprolactame, Phenole und Hydroxam­säureester. Bevorzugte Blockierungsmittel sind Malon­ester, Acetessigester und β-Diketone.Any suitable aliphatic, cycloaliphatic or aromatic alkyl mono alcohols can be used to block the polyisocyanates. Examples include aliphatic alcohols such as methyl, ethyl, chloroethyl, propyl, butyl, amyl, hexyl, heptyl, octyl, nonyl, 3,3,5-trimethylhexyl, decyl and lauryl alcohol ; aromatic alkyl alcohols such as phenylcarbinol and methylphenylcarbinol. It is also possible, if appropriate, to use small proportions of higher molecular weight and relatively low-volatility monoalcohols, these alcohols acting as plasticizers in the coatings after they have been split off.
Other suitable blocking agents are oximes, such as methyl ethyl ketone oxime, acetone oxime and cyclohexanone oxime, as well as caprolactams, phenols and hydroxamic acid esters. Preferred blocking agents are malonic esters, acetoacetic esters and β-diketones.

Die blockierten Polyisocyanate werden hergestellt, indem man eine ausreichende Menge eines Alkohols mit dem organischen Polyisocyanat umsetzt, so daß keine freien Isocyanatgruppen mehr vorhanden sind.The blocked polyisocyanates are produced by reacting a sufficient amount of an alcohol with the organic polyisocyanate so that there are no free isocyanate groups.

Die erfindungsgemäßen Basisbeschichtungszusammen­setzungen können alle bekannten und in der Lackin­dustrie üblichen Pigmente oder Farbstoffe enthalten.The base coating compositions according to the invention can contain all known pigments or dyes which are customary in the paint industry.

Als Farbstoffe bzw. Pigmente, die anorganischer oder organischer Natur sein können, werden beispiels­weise genannt Titandioxid, Graphit, Ruß, Zinkchromat, Strontriumchromat, Bariumchromat, Bleichromat, Blei­cyanamid, Bleisilicochromat, Zinkoxid, Cadmiumsulfid, Chromoxid, Zinksulfid, Nickeltitangelb, Chromtitan­gelb, Eisenoxidrot, Eisenoxidschwarz, Ultramarinblau, Phthalocyaninkomplexe, Naphtholrot, Chinacridone, halogenierte Thioindigo-Pigmente oder dergleichen.Dyes or pigments, which can be of an inorganic or organic nature, are, for example, titanium dioxide, graphite, carbon black, zinc chromate, strontrium chromate, barium chromate, lead chromate, lead cyanamide, lead silicochromate, zinc oxide, cadmium sulfide, Chromium oxide, zinc sulfide, nickel titanium yellow, chrome titanium yellow, iron oxide red, iron oxide black, ultramarine blue, phthalocyanine complexes, naphthol red, quinacridones, halogenated thioindigo pigments or the like.

Als besonders bevorzugte Pigmente werden Metallpulver einzeln oder im Gemisch wie Kupfer, Kupferlegierungen, Aluminium und Stahl, vorzugsweise Aluminiumpulver, in wenigstens überwiegendem Anteil eingesetzt, und zwar in einer Menge von 0,5 bis 25 Gew.-% bezogen auf den gesamten Festkörpergehalt der Überzugsmittel an Bindemitteln. Als metallische Pigmente werden solche handelsüblichen Metallpulver bevorzugt, die für wäßrige Systeme speziell vorbehandelt sind.
Die Metallpulver können auch zusammen mit einem oder mehreren der obengenannten nichtmetallischen Pigmente bzw. Farbstoffe eingesetzt werden. In diesem Fall wird deren Anteil so gewählt, daß der erwünschte Metallic-Effekt nicht unterdrück wird.As particularly preferred pigments, metal powders are used individually or in a mixture, such as copper, copper alloys, aluminum and steel, preferably aluminum powder, in at least a predominant proportion, namely in an amount of 0.5 to 25% by weight, based on the total solids content of the coating compositions on binders. Commercially available metal powders which are specially pretreated for aqueous systems are preferred as metallic pigments.
The metal powders can also be used together with one or more of the abovementioned non-metallic pigments or dyes. In this case, their proportion is chosen so that the desired metallic effect is not suppressed.

Die erfindungsgemäßen Basisbeschichtungszusammen­setzungen können auch weitere übliche Zusätze wie Lösungsmittel, Füllstoffe, Weichmacher, Stabilisatoren, Netzmittel, Dispergierhilfsmittel, Verlaufmittel, Entschäumer und Katalysatoren einzeln oder im Gemisch in den üblichen Mengen enthalten. Diese Substanzen können den Einzelkomponenten und/oder der Gesamtmischung zugesetzt werden.The base coating compositions according to the invention can also contain other customary additives, such as solvents, fillers, plasticizers, stabilizers, wetting agents, dispersing assistants, leveling agents, defoamers and catalysts, individually or in a mixture in the customary amounts. These substances can be added to the individual components and / or the overall mixture.

Geeignete Füllstoffe sind z.B. Talkum, Glimmer, Kaolin, Kreide, Quarzmehl, Asbestmehl, Schiefermehl, Barium­sulfat, verschiedene Kieselsäuren, Silikate, Glas­fasern, organische Fasern und dergleichen.
Die oben beschriebenen Beschichtungszusammensetzungen werden erfindungsgemäß in Verfahren zur Herstellung von mehrschichtigen Überzügen auf Substratoberflächen verwendet, bei welchen

  • (1) als Basisbeschichtungszusammensetzung eine wäßrige Dispersion aufgebracht wird
  • (2) aus der in Stufe (1) aufgebrachten Zusammensetzung ein Polymerfilm auf der Substratoberfläche gebildet wird
  • (3) auf der so erhaltenen Basisschicht eine geeignete transparente Deckschichtzusammensetzung aufge­bracht und anschließend
  • (4) die Basisschicht zusammen mit der Deckschicht einge­brannt wird.
Suitable fillers are, for example, talc, mica, kaolin, chalk, quartz flour, asbestos flour, slate flour, barium sulfate, various silicas, silicates, glass fibers, organic fibers and the like.
The coating compositions described above are used according to the invention in processes for the production of multilayer coatings on substrate surfaces, in which
  • (1) an aqueous dispersion is applied as the base coating composition
  • (2) a polymer film is formed on the substrate surface from the composition applied in step (1)
  • (3) a suitable transparent cover layer composition is applied to the base layer thus obtained and then
  • (4) the base layer is baked together with the cover layer.

Als Deckschichtzusammensetzungen sind grundsätzlich alle bekannten nicht oder nur transparent pigmentierten Überzugsmittel geeignet. Hierbei kann es sich um konven­tionelle lösungsmittelhaltige Klarlacke, wasserverdünn­bare Klarlacke oder Pulverklarlacke handeln.In principle, all known coating compositions which are not pigmented or only transparent pigmented are suitable as top layer compositions. These can be conventional solvent-borne clearcoats, water-borne clearcoats or powder clearcoats.

Als zu beschichtende Substrate kommen vor allem vor­behandelte Metallsubstrate in Frage, es können aber auch nicht vorbehandelte Metalle und beliebige andere Substrate wie zum Beispiel Holz, Kunststoffe u.s.w. unter Verwendung der erfindnugsgemäßen Basisbe­schichtungszusammensetzungen mit einer mehrschichtigen schützenden und/oder dekorativen Beschichtung über­zogen werden.Pretreated metal substrates are particularly suitable as substrates, but non-pretreated metals and any other substrates such as wood, plastics etc. can also be used. can be coated with a multilayer protective and / or decorative coating using the base coating compositions according to the invention.

Die Erfindung wird in den folgenden Beispielen näher erläutert. Alle Angaben über Teile und Prozentsätze sind Gewichtsangaben, falls nicht ausdrücklich etwas anderes festgestellt wird.The invention is explained in more detail in the following examples. All parts and percentages are by weight unless expressly stated otherwise.

Herstellung einer erfindungsgemäßen PolyurethandispersionPreparation of a polyurethane dispersion according to the invention

255 g eines Polyesters aus Hexandiol-1,6 und Isophthal­säure mit einem mittleren Molekulargewicht von 614, werden zusammen mit 248 g eines Polypropylenglykols mit einem mittleren Molekulargewicht von 600 und mit 100 g Dimethylolpropionsäure auf 100°C erhitzt und 1 Stunde im Vakuum entwässert. Bei 80°C werden 526 g 4,4ʹ-Dicyclohexylmethandiisocyanat und 480 g Methylethyl­keton zugegeben. Es wird bei 80°C so lange gerührt, bis der Gehalt an freien Isocyanatgruppen 1,69 %, bezo­gen auf die Gesamteinwaage, beträgt.255 g of a polyester of 1,6-hexanediol and isophthalic acid with an average molecular weight of 614 are heated to 100 ° C. together with 248 g of a polypropylene glycol with an average molecular weight of 600 and with 100 g of dimethylolpropionic acid Dewatered in a vacuum for 1 hour. 526 g of 4,4'-dicyclohexylmethane diisocyanate and 480 g of methyl ethyl ketone are added at 80 ° C. The mixture is stirred at 80 ° C. until the free isocyanate group content is 1.69%, based on the total weight.

Jetzt werden 28,5 g Trimethylolpropan und anschließend 0,4 g Dibutylzinndilaurat zugegeben und 2 Stunden bei 80°C weiter gerührt. Nach Zugabe von 1590 g Methylethyl­keton wird so lange bei 80°C gehalten, bis die Viskosi­tät, gemessen im DIN-Becher, 65 s beträgt (Probe im Verhältnis 2:3 in N-Methylpyrrolidon gelöst).Now 28.5 g of trimethylolpropane and then 0.4 g of dibutyltin dilaurate are added and stirring is continued at 80 ° C. for 2 hours. After adding 1590 g of methyl ethyl ketone, the mixture is kept at 80 ° C. until the viscosity, measured in a DIN beaker, is 65 s (sample dissolved in N: methylpyrrolidone in a ratio of 2: 3).

Nach Zugabe einer Mischung aus 22,4 g Dimethyletha­nolamin und 2650 g deionisiertem Wasser wird im Vakuum das Methylethylketon abdestilliert, und man erhält eine feinteilige Dispersion mit einem Festkörpergehalt von 30 %, einem pH-Wert von 7,4 und einer Viskosität von 48 s, gemessen im DIN-Becher.After adding a mixture of 22.4 g of dimethylethanolamine and 2650 g of deionized water, the methyl ethyl ketone is distilled off in vacuo, and a finely divided dispersion with a solids content of 30%, a pH of 7.4 and a viscosity of 48 s is obtained. measured in a DIN cup.

Herstellung von Zweischicht-Lackierungen nach dem Base-Coat-/Clear-Coat-Verfahren unter Verwendung der nach obiger Vorschrift hergestellten erfindungsgemäßen PolyurethandispersionProduction of two-layer coatings by the base coat / clear coat method using the polyurethane dispersion according to the invention produced according to the above regulation

Die Herstellung der Zweischichtlackierung erfolgte nach den in der US 4, 558, 090 angegebenen experimen­tellen Angaben.The two-layer coating was produced in accordance with the experimental information given in US Pat. No. 4,558,090.

Ein unter Verwendung der erfindungsgemäßen Polyurethan­dispersion hergestellter Metalleffekt-Basislack konnte zu einer qualitativ hochwertigen zweischichtigen Metall­effektlackierung mit einem ausgezeichneten Metalleffekt verarbeitet werden.A metallic effect basecoat produced using the polyurethane dispersion according to the invention could be processed into a high-quality two-layer metallic effect coating with an excellent metallic effect.

Die Entfernbarkeit von in den Applikationsgeräten zurück­gebliebenen Lackresten wird anhand der folgenden Ver­gleichsversuche demonstriert:
Auf einer Glasplatte wurde ein Metalleffekt-Basislack gemäß der US 4,558,090 und ein Metalleffekt-Basislack gemäß der vorliegenden Erfindung in einer Naßfilmdicke von 100 µm mit Hilfe eines Rakels aufgetragen.The removability of paint residues remaining in the application devices is demonstrated using the following comparison tests:
A metal-effect basecoat according to US Pat. No. 4,558,090 and a metal-effect basecoat according to the present invention were applied to a glass plate in a wet film thickness of 100 μm using a doctor blade.

Nach 2stündigem Trocknen bei Raumtemperatur wurde mit einer Mischung auf 50 Teilen Wasser und 50 Teilen n-Pro­panol versucht, den angetrockneten Lackfilm von der Glasplatte zu entfernen. Dazu wurde ein mit dieser Reinigungsmischung getränkter Pinsel mit leichtem Druck in kreisenden Bewegungen über den getrockneten Lackfilm geführt. Der aus dem erfindungsgemäß hergestellten Metalleffekt-Basislack gebildete Lackfilm löste sich schon nach den ersten Kreisbewegungen homogen auf. Der unter Verwendung der in der US 4,558,090 offenbarten Dispersion hergestellte Lackfilm dagegen quoll zunächst auf und löste sich erst nach vielfachen Kreisbewegungen in größeren zusammenhängenden Fladen vom Untergrund ab.After drying for 2 hours at room temperature, a mixture with 50 parts of water and 50 parts of n-propanol was used to try to remove the dried lacquer film from the glass plate. For this purpose, a brush soaked with this cleaning mixture was passed over the dried paint film in a circular motion with light pressure. The paint film formed from the metallic effect basecoat produced according to the invention dissolved homogeneously after the first circular movements. The paint film produced using the dispersion disclosed in US Pat. No. 4,558,090, on the other hand, initially swelled and only detached from the substrate after numerous circular movements in larger, coherent flat sheets.

Dieser Versuch wurde mit einer Vielzahl unterschiedlich­ster Lösungsmittel bzw. Lösungsmittelgemische wieder­holt. In allen Fällen wurden ähnliche Ergebnisse erhal­ten.This experiment was repeated with a large number of different solvents or solvent mixtures. Similar results were obtained in all cases.

Claims (10)

1. Basisbeschichtungszusammensetzung zur Herstellung von mehrschichtigen, schützenden und/oder dekora­tiven Überzügen bestehend aus einer wässrigen Dispersion, die
(a) als filmbildendes Material mindestens ein Poly­urethanharz mit einer Säurezahl von 5 bis 70, welches hergestellt worden ist, indem aus
(A) linearen Polyether- und/oder Polyesterdiolen mit einem Molekulargewicht von 400 bis 3000
(B) Diisocyanaten und
(C) Verbindungen, die zwei gegenüber Isocyanat­gruppen reaktive Gruppen enthalten, wobei zumindest ein Teil der als Komponente (C) eingesetzten Verbindungen mindestens eine zur Anionenbildung befähigte Gruppe aufweist, die vorzugsweise vor der Umsetzung mit einem tertiären Amin neutralisiert worden ist,
ein endständige Isocyanatgruppen aufweisendes Zwischen­produkt hergestellt worden ist, dessen freie Isocyanat­gruppen anschließend mit
(D) weiteren, gegenüber Isocyanatgruppen reaktive Gruppen enthaltenden Verbindungen
umgesetzt worden sind
(b) Pigmente und
(c) weitere übliche Additive
enthält
dadurch gekennzeichnet, daß
die wässrige Polyurethandispersion durch Umsetzung des aus (A), (B) und (C) erhaltenen Zwischenproduktes mit einem mindestens drei Hydroxylgruppen enthaltenden Polyol, vorzugsweise Triol, und Überführung des so gewonnenen Reaktionsproduktes in eine wässrige Phase hergestellt worden ist.1. Base coating composition for the production of multilayer, protective and / or decorative coatings consisting of an aqueous dispersion, the
(a) as film-forming material at least one polyurethane resin with an acid number of 5 to 70, which has been produced by
(A) linear polyether and / or polyester diols with a molecular weight of 400 to 3000
(B) diisocyanates and
(C) compounds which contain two groups which are reactive toward isocyanate groups, at least some of the compounds used as component (C) having at least one group capable of forming anions which has preferably been neutralized before the reaction with a tertiary amine,
an intermediate product having terminal isocyanate groups has been prepared, the free isocyanate groups of which are then also present
(D) further compounds containing groups reactive toward isocyanate groups
have been implemented
(b) pigments and
(c) other common additives
contains
characterized in that
the aqueous polyurethane dispersion has been prepared by reacting the intermediate product obtained from (A), (B) and (C) with a polyol containing at least three hydroxyl groups, preferably triol, and converting the reaction product thus obtained into an aqueous phase. 2. Verfahren zur Herstellung eines mehrschichtigen, schützenden und/oder dekorativen Überzuges auf einer Substratoberfläche, bei welchem
(1) als Basisbeschichtungszusammensetzung eine wässrige Dispersion aufgebracht wird, die
(a) als filmbildendes Material mindestens eine Polyurethanharz mit einer Säurezahl von 5 bis 70, welches hergestellt worden ist, indem aus
(A) linearen Polyether- und/oder Polyester­diolen mit einem Molekulargewicht von 400 bis 3000
(B) Diisocyanaten und
(C) Verbindungen, die zwei gegenüber Iso­cyanatgruppen reaktive Gruppen enthalten, wobei zumindest ein Teil der als Kompo­nente (C) eingesetzten Verbindungen mindestens eine zur Anionenbildung befähigte Gruppe aufweist, die vorzugs­weise vor der Umsetzung mit einem tertiären Amin neutralisiert worden ist
ein endständige Isocyanatgruppen aufweisendes Zwischen­produkt hergestellt worden ist, dessen freie Isocyanat­gruppen anschließend mit
(D) weiteren, gegenüber Isocyanatgruppen reaktive Gruppen enthaltenden Verbin­dungen
umgesetzt worden sind,
(b) Pigmente und
(c) weitere übliche Additive enthält.
(2). Aus der in Stufe (1) aufgebrachten Zusammen­setzung ein Polymerfilm auf der Oberfläche gebildet wird,
(3) auf der so erhaltenen Basisschicht eine geeig­nete transparente Deckschichtzusammensetzung aufgebracht und anschließend die Basisschicht zusammen mit der Deckschicht eingebrannt wird,
dadurch gekennzeichnet, daß
die die Basisbeschichtungszusammensetzung bildende Polyurethandispersion durch eine Umsetzung des aus (A), (B) und (C) erhaltenen Zwischenproduktes mit einem mindestens drei Hydroxylgruppen enthaltenden Polyol, vorzugsweise Triol, und Überführung des so gewonnenen Reaktionsproduktes in die wässrige Phase hergestellt worden ist.2. A method for producing a multilayer, protective and / or decorative coating on a substrate surface, in which
(1) an aqueous dispersion is applied as the base coating composition, which
(a) as film-forming material at least one polyurethane resin with an acid number of 5 to 70, which has been produced by
(A) linear polyether and / or polyester diols with a molecular weight of 400 to 3000
(B) diisocyanates and
(C) Compounds which contain two groups which are reactive toward isocyanate groups, at least some of the compounds used as component (C) having at least one group capable of forming anions which has preferably been neutralized before the reaction with a tertiary amine
an intermediate product having terminal isocyanate groups has been prepared, the free isocyanate groups of which are then also present
(D) further compounds containing groups reactive toward isocyanate groups
have been implemented
(b) pigments and
(c) contains other conventional additives.
(2). A polymer film is formed on the surface from the composition applied in step (1),
(3) a suitable transparent top layer composition on the base layer thus obtained applied and then the base layer is baked together with the cover layer,
characterized in that
the polyurethane dispersion forming the base coating composition has been prepared by reacting the intermediate product obtained from (A), (B) and (C) with a polyol containing at least three hydroxyl groups, preferably triol, and converting the reaction product thus obtained into the aqueous phase. 3. Basisbeschichtungszusammensetzung oder Verfahren nach den Ansprüchen 1 oder 2
dadurch gekennzeichnet, daß
die Umsetzung des aus (A), (B) und (C) erhaltenen Zwischenproduktes mit dem Polyol in einem wasser­mischbaren, unter 100 °C siedenden gegenüber Isocyanatgruppen inerten und aus wässrigen Mischungen gut abtrennbaren organischen Lösungs­mittel, bevorzugt Aceton, durchgeführt worden ist.3. Base coating composition or method according to claims 1 or 2
characterized in that
the reaction of the intermediate product obtained from (A), (B) and (C) with the polyol has been carried out in a water-miscible organic solvent, preferably acetone, which is inert towards isocyanate groups and boils below 100 ° C. and can be separated off from aqueous mixtures. 4. Basisbeschichtungszusammensetzung oder Verfahren nach einem der Ansprüche 1 bis 3
dadurch gekennzeichnet, daß
das aus (A), (B) und (C) erhaltene Zwischenprodukt mit Trimethylolpropan umgesetzt worden ist.4. Base coating composition or method according to one of claims 1 to 3
characterized in that
the intermediate obtained from (A), (B) and (C) has been reacted with trimethylolpropane. 5. Basisbeschichtungszusammensetzung oder Verfahren nach einem der Ansprüche 1 bis 4
dadurch gekennzeichnet, daß
die Basisbeschichtungszusammensetzung als zusätzliche Bindemittelkomponente ein wasserverdünnbares Melamin­harz in einem Anteil von 1 bis 80 Gew.-%, bevorzugt 20 bis 60 Gew.-%, bezogen auf den Festkörpergehalt der Polyurethandispersion, enthält.5. Base coating composition or method according to one of claims 1 to 4
characterized in that
the base coating composition contains, as an additional binder component, a water-dilutable melamine resin in a proportion of 1 to 80% by weight, preferably 20 to 60% by weight, based on the solids content of the polyurethane dispersion. 6. Basisbeschichtungszusammensetzung oder Verfahren nach einem der Ansprüche 1 bis 5
dadurch gekennzeichnet, daß
die Basisbeschichtungszusammensetzung als weitere Bindemittelkomponente ein wasserverdünnbares Polyesterharz und/oder ein wasserverdünnbares Polyacrylatharz enthält, wobei das Gewichtsver­hältnis Melaminharz zu Polyesterharz und/oder Polyacrylatharz 2:1 bis 1:4 beträgt und der Gesamt­anteil an Melaminharz, Polyester und Polyacrylat­harz, bezogen auf den Festkörpergehalt der Poly­urethandispersion, 1 bis 80 Gew.-%, bevorzugt 20 bis 60 Gew.-% beträgt.6. Base coating composition or method according to one of claims 1 to 5
characterized in that
the base coating composition contains, as a further binder component, a water-dilutable polyester resin and / or a water-dilutable polyacrylate resin, the weight ratio of melamine resin to polyester resin and / or polyacrylate resin being 2: 1 to 1: 4 and the total proportion of melamine resin, polyester and polyacrylate resin, based on the solids content of the polyurethane dispersion , 1 to 80 wt .-%, preferably 20 to 60 wt .-%. 7. Basisbeschichtungszusammensetzung oder Verfahren nach einem der Ansprüche 1 bis 6
dadurch gekennzeichnet, daß
die Basisbeschichtungszusammensetzung als zusätzliche Bindemittelkomponente ein blockiertes Polyisocyanat, zusammen mit einem wasserverdünnbaren Polyesterharz und/oder einem wasserverdünnbaren Polyacrylatharz, enthält, wobei der Anteil an Polyisocyanat, Poly­esterharz, und/oder Polyacrylatharz insgesamt 1 bis 80 Gew.-%, bezogen auf den Festkörpergehalt der Polyurethandispersion, beträgt.7. Base coating composition or method according to one of claims 1 to 6
characterized in that
the base coating composition contains, as an additional binder component, a blocked polyisocyanate, together with a water-dilutable polyester resin and / or a water-dilutable polyacrylate resin, the proportion of polyisocyanate, polyester resin and / or polyacrylate resin totaling 1 to 80% by weight, based on the solids content of the polyurethane dispersion , is. 8. Basisbeschichtungszusammensetzung oder Verfahren nach einem der Ansprüche 1 bis 7
dadurch gekennzeichnet, daß
die Basisbeschichtungszusammensetzung 0,5 bis 25 Gew.-% Metallpigmente, bezogen auf den gesamten Festkörpergehalt der Polyurethandispersion, enthält.8. Base coating composition or method according to one of claims 1 to 7
characterized in that
the basecoat composition 0.5 to Contains 25 wt .-% metal pigments, based on the total solids content of the polyurethane dispersion. 9. Verwendung von wässrigen Dispersionen, die
(a) als filmbildendes Material mindestens ein Polyurethanharz mit einer Säurezahl von 5 bis 70, welches hergestellt worden ist, indem aus
(A) linearen Polyether- und/oder Polyester­diolen mit einem Molekulargewicht von 400 bis 3000
(B) Diisocyanaten und
(C) Verbindungen, die zwei gegenüber Iso­cyanatgruppen reaktive Gruppen enthalten, wobei zumindest ein Teil der als Kompo­nente (C) eingesetzten Verbindungen mindestens eine zur Anionenbildung be­fähigte Gruppe aufweist, die vorzugsweise vor der Umsetzung mit einem tertiären Amin neutralisiert worden ist,
ein endständige Isocyanatgruppen aufweisendes Zwischenprodukt hergestellt worden ist, dessen freie Isocyanatgruppen anschließend mit einem mindestens drei Hydroxylgruppen enthaltenden Polyol, vorzugsweise Triol, umgesetzt worden sind,
(b) Pigmente und
(c) weitere übliche Additive
enthalten, als Basisbeschichtungszusammensetzungen für die Herstellung von mehrschichtigen, schützenden und/oder dekorativen Überzügen auf Substratober­flächen.9. Use of aqueous dispersions
(a) as film-forming material at least one polyurethane resin with an acid number of 5 to 70, which has been produced by
(A) linear polyether and / or polyester diols with a molecular weight of 400 to 3000
(B) diisocyanates and
(C) compounds which contain two groups which are reactive toward isocyanate groups, at least some of the compounds used as component (C) having at least one group capable of forming anions which has preferably been neutralized before the reaction with a tertiary amine,
an intermediate product having terminal isocyanate groups has been prepared, the free isocyanate groups of which have subsequently been reacted with a polyol containing at least three hydroxyl groups, preferably triol,
(b) pigments and
(c) other common additives
contain, as a base coating compositions for the production of multilayer, protective and / or decorative coatings on substrate surfaces. 10. Substrat, beschichtet mit einem mehrschichtigen, schützenden und/oder dekorativem Überzug, der erhalten worden ist, indem (1) als Basisbeschichtungszusammensetzung eine wässrige Dispersion aufgebracht worden ist, die
(a) als filbildendes Material mindestens ein Polyurethanharz mit einer Säurezahl von 5 bis 70, welches hergestellt worden ist, indem aus
(A) linearen Polyether und/oder Polyester­diolen mit einem Molekulargewicht von 400 bis 3000
(B) Diisocyanaten und
(C) Verbindungen, die zwei gegenüber Isocyanat­gruppen reaktive Gruppen enthalten, wobei zumindest ein Teil der als Kompo­nente (C) eingesetzten Verbindungen mindestens eine zur Anionenbildung be­fähigte Gruppe aufweist, die vorzugsweise vor der Umsetzung mit einem tertiären Amin neutralisiert worden ist,
ein endständige Isocyanatgruppen aufweisendes Zwischen­produkt hergestellt worden ist, dessen freie Isocyanat­gruppen anschließend mit
(D) weiteren, gegenüber Isocyanatgruppen reaktive Gruppen enthaltenden Verbindungen umgesetzt worden sind
(b) Pigmente und
(c) weitere übliche Additve enthält. (2) aus der in Stufe (1) aufgebrachten Zusammen­setzung ein Polymerfilm auf der Oberfläche gebildet worden ist, (3) auf der so erhaltenen Basisschicht eine geeignete transparente Deckschicht-Zusammensetzung aufgebracht worden ist und anschließend (4) die Basisschicht zusammen mit der Deckschicht eingebrannt worden ist,
dadurch gekennzeichnet, daß
die die Basisbeschichtungszusammensetzung bildende wässrige Polyurethandispersion durch eine Umsetzung des aus (A), (B) und (C) erhaltenen Zwischenproduktes mit einem mindestens drei Hydroxylgruppen enthaltenden Polyol, vorzugsweise Triol, und Überführung des so gewonnenen Reaktionsproduktes in eine wässrige Phase hergestellt worden ist. 10. Substrate coated with a multilayer, protective and / or decorative coating which has been obtained by (1) An aqueous dispersion has been applied as the base coating composition
(a) as a film-forming material at least one polyurethane resin with an acid number of 5 to 70, which has been produced by
(A) linear polyethers and / or polyester diols with a molecular weight of 400 to 3000
(B) diisocyanates and
(C) compounds which contain two groups which are reactive toward isocyanate groups, at least some of the compounds used as component (C) having at least one group capable of forming anions which has preferably been neutralized before the reaction with a tertiary amine,
an intermediate product having terminal isocyanate groups has been prepared, the free isocyanate groups of which are then also present
(D) further compounds containing groups reactive toward isocyanate groups have been reacted
(b) pigments and
(c) contains further conventional additives. (2) a polymer film has been formed on the surface from the composition applied in step (1), (3) a suitable transparent cover layer composition has been applied to the base layer thus obtained and then (4) the base layer has been baked together with the cover layer,
characterized in that
the aqueous polyurethane dispersion forming the base coating composition has been prepared by reacting the intermediate product obtained from (A), (B) and (C) with a polyol containing at least three hydroxyl groups, preferably triol, and converting the reaction product thus obtained into an aqueous phase.
EP86117295A 1985-12-21 1986-12-11 Preparation of a multilayer coating Expired - Lifetime EP0228003B2 (en)

Priority Applications (1)

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AU600254B2 (en) 1990-08-09
ATE51633T1 (en) 1990-04-15
EP0228003B1 (en) 1990-04-04
CA1307611C (en) 1992-09-15
ES2014979T5 (en) 1995-08-16
DE3670089D1 (en) 1990-05-10
BR8607234A (en) 1988-11-01
ES2014979B3 (en) 1990-08-01
US4914148A (en) 1990-04-03
AU6842787A (en) 1987-07-15
ZA869378B (en) 1987-09-30
JPS63502755A (en) 1988-10-13
WO1987003829A1 (en) 1987-07-02
EP0228003B2 (en) 1994-03-23
EP0279813A1 (en) 1988-08-31
DE3545618A1 (en) 1987-06-25

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